First published online April 23, 2004; 10.1104/pp.103.038430
Plant Physiology 135:103-111 (2004)
© 2004 American Society of Plant Biologists
BIOCHEMICAL PROCESSES AND MACROMOLECULAR STRUCTURES
Folate Biosynthesis in Higher Plants. cDNA Cloning, Heterologous Expression, and Characterization of Dihydroneopterin Aldolases1,[w]
Aymeric Goyer2,
Victoria Illarionova2,
Sanja Roje2,
Markus Fischer,
Adelbert Bacher and
Andrew D. Hanson*
Horticultural Sciences Department, University of Florida, Gainesville, Florida 32611 (A.G., S.R., A.D.H.); and Lehrstuhl für Organische Chemie und Biochemie, Technische Universität München, D85747 Garching, Germany (V.I., M.F., A.B)
Dihydroneopterin aldolase (EC 4.1.2.25) is one of the enzymes of folate synthesis that remains to be cloned and characterized from plants. This enzyme catalyzes conversion of 7,8-dihydroneopterin (DHN) to 6-hydroxymethyl-7,8-dihydropterin, and is encoded by the folB gene in Escherichia coli. The E. coli FolB protein also mediates epimerization of DHN to 7,8-dihydromonapterin. Searches of the Arabidopsis genome detected three genes encoding substantially diverged FolB homologs (AtFolB13, sharing 57%73% identity), for which cDNAs were isolated. A fourth cDNA specifying a FolB-like protein (LeFolB1) was obtained from tomato (Lycopersicon esculentum) by reverse transcription-PCR. When overproduced in E. coli, recombinant AtFolB1, AtFolB2, and LeFolB1 proteins all had both dihydroneopterin aldolase and epimerase activities, and carried out the aldol cleavage reaction on the epimerization product, 7,8-dihydromonapterin, as well as on DHN. AtFolB3, however, could not be expressed in active form. Size exclusion chromatography indicated that the plant enzyme is an octamer, like the bacterial enzyme. Quantifying expression of the Arabidopsis genes by real-time reverse transcription-PCR showed that AtFolB1 and AtFolB2 messages occur at low levels throughout the plant, whereas the AtFolB3 mRNA was detected only in siliques and only with an extremely low abundance. Sequence comparisons and phylogenetic analysis of FolB homologs from 16 plants indicated that their N-terminal regions are highly variable, and that most species have a small number of FolB genes that diverged after separation of the lineages leading to families. The substantial divergence of FolB homologs in Arabidopsis and other plants suggests that some of them may act on substrates other than DHN.
1 This work was supported in part by the National Science Foundation (grant no. MCB0129944); by the Deutsche Forschungsgemeinschaft, the Fonds der Chemischen Industrie, and the Hans-Fischer-Gesellschaft; by an endowment from the C.V. Griffin, Sr. Foundation; and by the Florida Agricultural Experiment Station. Journal Series No. R-09930.
2 These authors contributed equally to the paper.
[w] The online version of this article contains Web-only data.
Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.103.038430.
* Corresponding author; e-mail adha{at}mail.ifas.ufl.edu; fax 3523925653.
Received December 24, 2003;
returned for revision February 18, 2004;
accepted February 22, 2004.
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